Probiotic supplementation during antibiotic treatment is unjustified in maintaining the gut microbiome diversity: a systematic review and meta-analysis.


Journal

BMC medicine
ISSN: 1741-7015
Titre abrégé: BMC Med
Pays: England
ID NLM: 101190723

Informations de publication

Date de publication:
19 07 2023
Historique:
received: 07 02 2023
accepted: 26 06 2023
medline: 21 7 2023
pubmed: 20 7 2023
entrez: 19 7 2023
Statut: epublish

Résumé

Probiotics are often used to prevent antibiotic-induced low-diversity dysbiosis, however their effect is not yet sufficiently summarized in this regard. We aimed to investigate the effects of concurrent probiotic supplementation on gut microbiome composition during antibiotic therapy. We performed a systematic review and meta-analysis of randomized controlled trials reporting the differences in gut microbiome diversity between patients on antibiotic therapy with and without concomitant probiotic supplementation. The systematic search was performed in three databases (MEDLINE (via PubMed), Embase, and Cochrane Central Register of Controlled Trials (CENTRAL)) without filters on 15 October 2021. A random-effects model was used to estimate pooled mean differences (MD) with 95% confidence intervals (CI). This review was registered on PROSPERO (CRD42021282983). Of 11,769 identified articles, 15 were eligible in the systematic review and 5 in the meta-analyses. Quantitative data synthesis for Shannon (MD = 0.23, 95% CI: [(-)0.06-0.51]), Chao1 (MD = 11.59 [(-)18.42-41.60]) and observed OTUs (operational taxonomic unit) (MD = 17.15 [(-)9.43-43.73]) diversity indices revealed no significant difference between probiotic supplemented and control groups. Lacking data prevented meta-analyzing other diversity indices; however, most of the included studies reported no difference in the other reported α- and ß-diversity indices between the groups. Changes in the taxonomic composition varied across the eligible studies but tended to be similar in both groups. However, they showed a potential tendency to restore baseline levels in both groups after 3-8 weeks. This is the first meta-analysis and the most comprehensive review of the topic to date using high quality methods. The limited number of studies and low sample sizes are the main limitations of our study. Moreover, there was high variability across the studies regarding the indication of antibiotic therapy and the type, dose, and duration of antimicrobials and probiotics. Our results showed that probiotic supplementation during antibiotic therapy was not found to be influential on gut microbiome diversity indices. Defining appropriate microbiome diversity indices, their standard ranges, and their clinical relevance would be crucial.

Sections du résumé

BACKGROUND
Probiotics are often used to prevent antibiotic-induced low-diversity dysbiosis, however their effect is not yet sufficiently summarized in this regard. We aimed to investigate the effects of concurrent probiotic supplementation on gut microbiome composition during antibiotic therapy.
METHODS
We performed a systematic review and meta-analysis of randomized controlled trials reporting the differences in gut microbiome diversity between patients on antibiotic therapy with and without concomitant probiotic supplementation. The systematic search was performed in three databases (MEDLINE (via PubMed), Embase, and Cochrane Central Register of Controlled Trials (CENTRAL)) without filters on 15 October 2021. A random-effects model was used to estimate pooled mean differences (MD) with 95% confidence intervals (CI). This review was registered on PROSPERO (CRD42021282983).
RESULTS
Of 11,769 identified articles, 15 were eligible in the systematic review and 5 in the meta-analyses. Quantitative data synthesis for Shannon (MD = 0.23, 95% CI: [(-)0.06-0.51]), Chao1 (MD = 11.59 [(-)18.42-41.60]) and observed OTUs (operational taxonomic unit) (MD = 17.15 [(-)9.43-43.73]) diversity indices revealed no significant difference between probiotic supplemented and control groups. Lacking data prevented meta-analyzing other diversity indices; however, most of the included studies reported no difference in the other reported α- and ß-diversity indices between the groups. Changes in the taxonomic composition varied across the eligible studies but tended to be similar in both groups. However, they showed a potential tendency to restore baseline levels in both groups after 3-8 weeks. This is the first meta-analysis and the most comprehensive review of the topic to date using high quality methods. The limited number of studies and low sample sizes are the main limitations of our study. Moreover, there was high variability across the studies regarding the indication of antibiotic therapy and the type, dose, and duration of antimicrobials and probiotics.
CONCLUSIONS
Our results showed that probiotic supplementation during antibiotic therapy was not found to be influential on gut microbiome diversity indices. Defining appropriate microbiome diversity indices, their standard ranges, and their clinical relevance would be crucial.

Identifiants

pubmed: 37468916
doi: 10.1186/s12916-023-02961-0
pii: 10.1186/s12916-023-02961-0
pmc: PMC10355080
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Meta-Analysis Systematic Review Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

262

Informations de copyright

© 2023. The Author(s).

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Auteurs

Anna Júlia Éliás (AJ)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Doctoral School of Health Sciences, Semmelweis University, Budapest, Hungary.

Viktória Barna (V)

Faculty of Health Sciences, Semmelweis University, Budapest, Hungary.

Cristina Patoni (C)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

Dóra Demeter (D)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Military Hospital Medical Centre, Hungarian Defense Forces, Budapest, Hungary.

Dániel Sándor Veres (DS)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Department of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.

Stefania Bunduc (S)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Fundeni Clinical Institute, Bucharest, Romania.

Bálint Erőss (B)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Institute of Pancreatic Diseases, Semmelweis University, Budapest, Hungary.
Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.

Péter Hegyi (P)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Institute of Pancreatic Diseases, Semmelweis University, Budapest, Hungary.
Institute for Translational Medicine, Medical School, University of Pécs, Pécs, Hungary.

László Földvári-Nagy (L)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary. foldvari-nagy.laszlo@semmelweis.hu.
Department of Morphology and Physiology, Faculty of Health Sciences, Semmelweis University, Budapest, Hungary. foldvari-nagy.laszlo@semmelweis.hu.

Katalin Lenti (K)

Centre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Department of Morphology and Physiology, Faculty of Health Sciences, Semmelweis University, Budapest, Hungary.

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